Canonical Allele Identifier: CA2638881055
Gene: NOG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56595041T>A , CM000679.2:g.56595041T>A GRCh38
NC_000017.10:g.54672402T>A , CM000679.1:g.54672402T>A GRCh37
NC_000017.9:g.52027401T>A NCBI36
NG_011958.1:g.6343T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*119T>A MANE Select ENSP00000328181.4:n.*119T>A
ENST00000332822.4:c.*119T>A ENSP00000328181.4:n.*119T>A
NM_005450.4:c.*119T>A NP_005441.1:n.*119T>A
NM_005450.6:c.*119T>A MANE Select NP_005441.1:n.*119T>A